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Journal Abstract Search

138 related items for PubMed ID: 1665760

  • 1.
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  • 3. Linkage study of dominantly inherited olivo-ponto-cerebellar atrophy (OPCA) and Holmes' ataxia.
    Sasaki H, Wakisaka A, Katoh T, Yoshida MC, Hamada T, Shima K, Matsuura T, Tashiro K.
    Jinrui Idengaku Zasshi; 1988 Dec; 33(4):423-38. PubMed ID: 3251076
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  • 4. [Peculiar forms of familial olivo-ponto-cerebellar atrophy (Menzel type) and Joseph disease; clinico-neuropathological study of two families with nosological considerations].
    Ikeda T.
    Seishin Shinkeigaku Zasshi; 1987 Dec; 89(4):245-81. PubMed ID: 3476971
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  • 6. The relationship of multiple system atrophy to sporadic olivopontocerebellar atrophy and other forms of idiopathic late-onset cerebellar atrophy.
    Gilman S, Quinn NP.
    Neurology; 1996 May; 46(5):1197-9. PubMed ID: 8628452
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  • 9. Machado-Joseph disease in New England: clinical description and distinction from the olivopontocerebellar atrophies.
    Sudarsky L, Corwin L, Dawson DM.
    Mov Disord; 1992 May; 7(3):204-8. PubMed ID: 1620136
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  • 10. Olivopontocerebellar atrophy.
    Choi IS, Lee MS, Kim WT, Choi KK.
    Yonsei Med J; 1988 May; 29(3):233-8. PubMed ID: 3195154
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  • 11. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea.
    Fox SH, Nieves A, Bergeron C, Lang AE.
    Mov Disord; 2003 Dec; 18(12):1550-4. PubMed ID: 14673899
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  • 12. Familial ataxia with extreme difference in age of clinical onset.
    Amit R, Granit G, Shapira Y.
    Neuropediatrics; 1986 Aug; 17(3):165-7. PubMed ID: 3463881
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  • 13. Olivopontocerebellar atrophy in a large Iakut kinship in eastern Siberia.
    Goldfarb LG, Chumakov MP, Petrov PA, Fedorova NI, Gajdusek DC.
    Neurology; 1989 Nov; 39(11):1527-30. PubMed ID: 2812335
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  • 14. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].
    Kojima S.
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1294-6. PubMed ID: 8174328
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  • 16. [Olivopontocerebellar atrophy as an important differential diagnosis in atactic gait disorders in elderly patients].
    Waespe W, Hayek J, Wichmann W, Bader JP.
    Schweiz Med Wochenschr; 1988 Jul 12; 118(27-28):1032-8. PubMed ID: 3166204
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  • 17. [Multivariate analysis of the clinical signs in late cortical cerebellar atrophy (LCCA) in Japan--compared with olivo-ponto-cerebellar atrophy (OPCA) and hereditary cortical cerebellar atrophy (HCCA)].
    Yanagimoto S, Takayanagi T, Hirayama K, Nakamura R, Yanagisawa N.
    Rinsho Shinkeigaku; 1992 Sep 12; 32(9):951-5. PubMed ID: 1300266
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  • 18. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Sep 12; 7(3):193-203. PubMed ID: 1620135
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  • 19. [Correlation of clinical course with MRI findings in olivo-pontocerebellar atrophy and late-cortical cerebellar atrophy].
    Konagaya M, Morishita S, Konagaya Y, Takayanagi T, Iwasaki S.
    Rinsho Shinkeigaku; 1989 Sep 12; 29(9):1122-9. PubMed ID: 2598538
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  • 20. Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.
    Kish SJ, Schut L, Simmons J, Gilbert J, Chang LJ, Rebbetoy M.
    J Neurol Neurosurg Psychiatry; 1988 Apr 12; 51(4):544-8. PubMed ID: 3164041
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